(Cephalopoda, Thysanoteuthidae) on the Brazilian coast - Biotaxa

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Geographic Distribution

Check List 10(4): 939–942, 2014 © 2014 Check List and Authors ISSN 1809-127X (available at www.checklist.org.br)

List

Journal of species lists and distribution

Geographic distribution of Thysanoteuthis rhombus (Cephalopoda, Thysanoteuthidae) on the Brazilian coast Carlo M. Cunha 1, 2* and Luciano E. Oliveira 3 1 2 3 *

Academy of Natural Sciences of Drexel University, Department of Malacology, 1900 Benjamin Franklin Parkway, Philadelphia, PA, USA 19103. Capes Foundation, Ministry of Education of Brazil, CEP 70040-020, Brasília, DF, Brazil. Terra Nativa Ecoturismo, Rua Manuel de Paiva, 257, CEP 04106-020, Vila Mariana, SP, Brazil. Corresponding author. E-mail: [email protected]

Abstract: Data on two female individuals of the diamonback squid, Thysanoteuthis rhombus, are presented with discussion of occurrences along the Brazilian coast. DOI: 10.15560/10.4.939

The diamondback squid, Thysanoteuthis rhombus Troschel, 1857, is a large (100–130 cm mantle length), muscular, nektonic squid. The mantle is think and muscular, tapering to a blunt tip posteriorly. The fins are long, broad, and rhombic in form and occupy the entire length of mantle. The tentacular clubs have four rows of suckers, arm with two rows of suckers, buccal connectives attached to ventral borders of arms IV (Roper and Jereb 2010). As unique species of the family Thysanoteuthidae Keferstein, 1866, this species is a common circumglobal inhabitant of warm tropical and subtropical open waters. This species was already recorded at India (Batcha et al. 2009), Sulawesi (Billings et al. 2000), the Aegean (Salman et al. 2003; Salman 2012), Adriatic Sea (Bello 2009), Arabian Mediterranean (Chesalin and Zuyev 2002) and Caribbean Sea (Pulido-Lopez and Lopez-Pinto 2002; Salvat-Torres et al. 2009; Roper and Jereb 2010). In the Atlantic Ocean, Thysanoteuthis rhombus occurs from latitude 30° N to 36° S and its southernmost distribution is bounded the displacement of the waters of the Brazilian Current (Brunetti et al. 1999). Thysanoteuthis rhombus has been known in Brazilian waters since 1985 but there is neither material deposited in scientific collections nor officially published records (Ferreira 1987). Records of both juvenile and adult individuals of T. rhombus from along the Brazilian coast are scarce, and for the Southern Atlantic Ocean, there are only three records in the literature (Haimovici et al. 1989; Haimovici and Perez 1991; Brunetti et al. 1999). Herein we report the presence of two adult specimens of the diamondback squid, T. rhombus, collected along the southern coast of Brazil. The two female specimens were captured and collected by longline vessel at Mostardas, Rio Grande do Sul, Brazil (31°40′00″ S 49°27′00″ W) and are housed at the mollusc collection of the Museu de Zoologia da Universidade de São Paulo (MZSP 97741 and MZSP 97740). Measurements follow Jereb et al. (2010) and were taken with a measuring tape and a scale. The samples were fixed in 10% formalin solution and preserved in 70% alcohol. Both specimens

possess similar measurements (Table 1) and represent the southern occurrence of the species on Brazil (Table 2) (Figure 1). Despite the length of the Brazilian coast and the 200 miles of exclusive economic area offshore, the capture of Thysanoteuthis rhombus adults (Figure 2) in this country is rare. These are incidental and are part of the bycatch of fisheries targeting the ommastrephid squid Ommastrephes bartramii (Lesueur, 1821) (Haimovici and Peres 1991). There is no directed fishing fleet for T. rhombus in Brazil. Nevertheless, T. rhombus has been considered as a target species with commercial interest in the Canary Islands (Báez and Marrero 2007; Pérez et al. 2012). In Japan, the annual catch increased from 339 tons in 1989 to almost 6000 tons in 2001, and during 1998–2003 the average catch was close to 4900 tons (Bower and Miyahara 2005). In Brazil, their presence was generally recorded indirectly by larvae (Nigmatullin et al. 1995; Haimovici et al. 2002) or stomach contents with beaks and partially digested specimens (Santos and Haimovici 2001, 2002; Vaske 2005; Vaske and Lessa 2005). Their low incidence is seen by the lack of representativeness in the stomachs of oceanic fishes (Vaske 2005; Leite et al. 2009). We observed that, despite the limited data available, distribution of mature individuals in the Atlantic South is connected to the Brazil Current, with northern and southern distribution between 23° and 36° S (Brunetti et al. 1999; Haimovici et al. 1989). The Brazil Current begins at about 10° S. Near 12° C the continental shelf becomes wider and this current separates slightly from the coast (Peterson and Stramma 1991). Here, Nigmatullin et al.

Table 1. Biometric data of the two adult specimens of Thysanoteuthis rhombus herein reported. BIOMETRIC DATA (cm) Total Length Mantle Length Arm Length Fin Length Head Width

MZUSP 97741 126 68 50 67 18

MZUSP 97740 125 62 53 64 18

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Cunha and Oliveira | Thysanoteuthis rhombus on the Brazilian coast

Table 2. Chronology of records of Thysanoteuthis rhombus in the Southern Atlantic Ocean. CAPTURE DATE

LOCATION

SOURCE

REMARKS

1 2 3

03/viii/1985 27/vii/1986 viii/1986

26°30′00″ S 45°52′30″ W 28°10′00″ S 46°39′00″ W 22°56′12″ S 42°28′51″ W

Ferreira 1987 Ferreira 1987 Haimovici et al. 1989

Captured by gill net at 9 m of fishing depth Captured by gill net at 55 m of fishing depth Captured by a fishermen at Itauna’s beach, Saquarema

5

1975-1990

northeast coast of Brazil

Nigmatullin et al. 1995

Larvae captured by zoological trawls and Isaacs-Kidd trawl at depth ranging from 0 to 100 m Confirmed the presence of the species in Argentine waters

4

6

1986-1987

iii/1999

Off Rio Grande do Sul 33° 30′ S 41° 30′ W

Haimovici and Perez 1991 Captured with a dipnet, at night with the ship stopped and deck lights were lit.

Brunetti et al. 1999

(1995) recorded T. rhombus larvae. The Brazil Current separation from the continental shelf varies anywhere between 33° S–38° S but it is usually about 36° S (Podesta et al., 1991), where it collides with the north-flowing Malvinas (Falkland) Current. The Brazil Current is then, in part, deflected offshore east of Rio de la Plata, a region known as the Brazil-Malvinas Confluence Zone (Saraceno et al. 2004). We conclude that the distribution of the Thysanoteuthis rhombus is south of the confluence zone between the Brazil and Malvinas Currents. We also conclude that the presence of adult individuals indicate that this species can breed in Brazilian waters.

Acknowledgements: We thank the crew of longline vessel QuebraMar provided the specimens studied, Ademir Guerreiro for his help with logistic processes; Dr. José E. Marian (Universidade de São Paulo, Brazil) for references; and, Robert Forsyth (subject editor for Check List) for the helpful comments. This work was partially supported by Fundação de amparo a Pesquisa do Estado de São Paulo (FAPESP) proc. #2010/112539 (CMC) and The Capes Foundation, Bolsista da CAPES proc. #8739/13-7 (CMC).

Literature Cited Báez, A. and M.F. Marrero. 2007. Manual de Identificación de las Principales Espécies Pesqueras. Gran Canaria: Excmo. Cabildo Insular de Gran Canaria. 112 pp. Batcha, H., R. Thangavelu, P. Poovannan and G. Srinivasan. 2009. Rare occurrence of diamond back squid Thysanoteuthis rhombus (Troschel, 1867) off Chennai coast. Indian Council of Agricultural Research Marine Fisheries Information Service Technical and Extension Series 201: 14–15. Bello, G. 2009. On the presence of Thysanoteuthis rhombus (Cephalopoda: Thysanoteuthidae) in the Adriatic Sea. Marine Biodiversity Records 2: 1–2 (doi: 10.1017/S1755267209990819). Billings, V.C., M. Sullivan and K. Vine. 2000. Sighting of Thysanoteuthis rhombus egg mass in Indonesian waters and observations of embryonic development. Journal of the Marine Biological Association of the United Kingdom 80(6): 1139–1140. Bower, J.R. and K. Miyahara. 2005. The diamond squid (Thysanoteuthis rhombus): A review of the fishery and recent research in Japan. Fisheries Research 73(1–2): 1–11 (doi: 10.1016%2Fj.fishres.2005.01.020.). Brunetti, N.E., M.L. Ivanovic and M. Sakai. 1999. Calamares de Importancia Comercial em La Argentina. Biología, Distribución, Pesquerias, Muestreo Biológico. Mar Del Plata: Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP). 45 pp. Chesalin, M.V. and G.V. Zuyev. 2002. Pelagic cephalopods of the Arabian Sea with an emphasis on Sthenoteuthis oualaniensis. Bulletin of Marine Science 71(1): 209–221. Ferreira, L.A. 1987. Primeiro registro de ocorrência da Lula Gigante Thysanoteuthis rhombus Troschell, 1857 no litoral brasileiro. In Programa e Resumos X Encontro Brasileiro de Malacologia SBM IBUSP. São Paulo: Universidade de São Paulo. Haimovici, M., J.A.A. Perez and P.A.S. Costa P.A.S. 1989. A review of cephalopods occurring in the waters of Rio de Janeiro State, Brazil with first record of four species. Revista Brasileira de Biologia 49(2): 503–510. Haimovici, M. and J.A.A. Perez. 1991. Abundância e distribuição de cefalópodes em cruzeiros de prospecção pesqueira demersal na plataforma externa e talude continental do Brasil. Atlântica 13(1): 189–200.

Figure 1. Distribution map of adult individuals of Thysanoteuthis rhombus catch in Brazil. Abbreviations: 1, Haimovici et al. 1989; 2 and 3, Ferreira 1987; 4, MZSP 97741 and MZSP 97740; RJ, Rio de Janeiro; SP, São Paulo; PR, Paraná; SC, Santa Catarina; RS, Rio Grande do Sul. Haimovici, M., U. Piatkowski and R.A. Santos. 2002. Cephalopod paralarvae around tropical seamounts and oceanic islands off the northeastern coast of Brazil. Bulletin of Marine Science 71(1): 313–330. Jereb, P., C.F.E. Roper and M. Vecchione. 2010. Introduction; pp. 1–11, in: P. Jereb and C.F.E. Roper (eds.). Cephalopods of the World. An Annotated and Illustrated Catalogue of Cephalopod Species Known to Date. Volume 2. Myopsid and Oegopsid Squids. Rome: FAO Species Catalogue for Fishery Purposes. Leite, T.S., L.C.A. Andrade, M. Haimovici, R.S. Aguiar and J.E.L. Oliveira. 2009. Lulas e polvos; pp. 138–147, 332–333, in: D.L. Vianda, F.H.V. Hazin and M.A.C. Souza (eds.). O Arquipélago de São Pedro e São Paulo: 10 anos de Estação Científica. Brasília: SECIRM. Nigmatullin, C.M., A.I. Arkhipkim and R.M. Sabirov. 1995. Age, growth and reproductive biology of diamond-shaped squid Thysanoteuthis rhombus (Oegopsida: Thysanoteuthidae). Marine Ecology Progress Series 124: 73–87. Pérez, A.E., R.R. Elena, Á.F. González and A.G. Sierra. 2012. On the occurrence of egg masses of the diamond-shaped squid Thysanoteuthis rhombusTroschel, 1857 in the subtropical eastern Atlantic (Canary Islands). A potential commercial species? ZooKeys 222: 69–76 (doi: 10.3897/zookeys.222.2835). Peterson, R.G. and L. Stramma. 1991. Upper-level circulation in the South Atlantic Ocean. Progress in Oceanography 26(1): 1–73. Podesta, G.P., O.B. Brown and R.H. Evans. 1991. The annual cycle of satellite-derived sea surface temperature in the Southwestern Atlantic Ocean. Journal of Climate 4:457–467 (doi: 10.1175/1520-0442(1991)004%3C0457:TACOSD%3E2.0.CO;2). Pulido-Lopez, P.C. and Y.A. Lopez-Pinto. 2002. First record of the diamond squid Thysanoteuthis rhombus Troschel, 1857 940

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Figure 2. Thysanoteuthis rhombus, MZSP 97741 (total length = 126 mm). A: Dorsal view. B: Same, ventral view. (Cephalopoda: Teuthida: Oegopsina) in the Colombian Caribbean Sea. Boletin de Investigaciones Marinas y Costeras 31:239–241 (http://www.scielo.org.co/scielo.php?script=sci_arttext&pid =S0122-97612002000100013). Roper, C.F.E. and P. Jereb. 2010. Family Thysanoteuthidae; pp. 384–387, in: P. Jereb, and C.F.E. Roper (eds.). Cephalopods of the World. An Annotated and Illustrated Catalogue of Cephalopod Species Known to Date. Volume 2. Myopsid and Oegopsid Squids. Rome: FAO Species Catalogue for Fishery Purposes. Salman A. 2012. Two new records of paralarva in the Eastern Mediterranean (Cephalopoda: Mollusca). Journal of the Black Sea/Mediterranean Environment 18(2): 197–207 (http://www. blackmeditjournal.org/pdf/vol18no2pdf9.pdf). Salman, A., T. Katagan and H.A. Benli. 2003. Vertical distribution and abundance of juvenile cephalopods in the Aegean Sea. Scientia Marina 67(2): 167–176 (http://www.icm.csic.es/scimar/download. php/Cd/f6315d7e5f1cdc667a900a0cc321079d/IdArt/3074). Salvat-Torres, H.M., L.C. Avila and M.G. Bermejo. 2009. A new record for the marine molluscs of Cuba: the diamond squid Thysanoteuthis rhombus (Mollusca: Cephalopoda). Revista de Investigaciones Marinas 30(3): 227–239 (http://www.cim.uh.cu/rim/pdf/2009/3/2009-237.pdf).

Santos, R.A. and M. Haimovici. 2001. Cephalopods in the diet of marine mammals stranded or incidentally caught along southeastern and southern Brazil (21–34°S). Fisheries Research 52(1): 99–112. Santos, R.A. and M. Haimovici. 2002. Cephalopods in the trophic relations off southern Brazil. Bulletin of Marine Science 71(2): 753–770. Saraceno, M., C. Provost, A.R. Piola, J. Bava and A. Gagliardini. 2004. Brazil Malvinas Frontal System as seen from 9 years of advanced very high resolution radiometer data. Journal of Geophysical Research 109(C5): C05027 (doi: 10.1029/2003JC002127). Vaske Jr. T. 2005. Cefalópodes oceânicos da zona econômica exclusiva do nordeste do Brasil. Boletim do Instituto de Pesca 31(2): 137–146. Vaske Jr., T. and R.P. Lessa. 2005. Estratégia alimentar do espadarte, Xiphias gladius, no Nordeste do Brasil. Tropical Oceanography 33(2): 219–217 (http://www.ufpe.br/tropicaloceanography/artigos_completos_ resumos_t_d/33_2005_2_vaske_jr.pdf). Received: January 2014 Accepted: June 2014 Published online: September 2014 Editorial responsibility: Robert G. Forsyth

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